Product Recalls in South Dakota

Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,330 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,330 in last 12 months

Showing 3438134400 of 47,632 recalls

Medical DeviceNovember 12, 2015· Corflex

Recalled Item: ADV ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-231...

The Issue: Knee brace could fail to maintain the locked position and a loss of balance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2015· Corflex

Recalled Item: CT ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-011 Post-Operative...

The Issue: Knee brace could fail to maintain the locked position and a loss of balance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2015· Corflex

Recalled Item: HAILEY ORTHO CONTENDER POST-OP-KNEE BRACE Model : 75-7500-038 Post-Operative...

The Issue: Knee brace could fail to maintain the locked position and a loss of balance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2015· Corflex

Recalled Item: ORTHO SPEC GRP CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-075...

The Issue: Knee brace could fail to maintain the locked position and a loss of balance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2015· Bestmed, LLC

Recalled Item: Digital Temple Thermometer labeled under: Bestmed Recalled by Bestmed, LLC...

The Issue: An incorrect calibration of the thermometer that causes the device to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugNovember 11, 2015· Fagron, Inc

Recalled Item: SyrSpend SF Recalled by Fagron, Inc Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· Fagron, Inc

Recalled Item: SyrSpend SF Recalled by Fagron, Inc Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· Fagron, Inc

Recalled Item: SyrSpend SF Recalled by Fagron, Inc Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Bicillin L-A 600000 Units/mL Inj. Recalled by RemedyRepack Inc. Due to...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Vitamin B-Complex 100 Recalled by RemedyRepack Inc. Due to Labeling:...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Ascorbic Acid 500 MG/ML Inj. Recalled by RemedyRepack Inc. Due to Labeling:...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Novolin 70/30 Recalled by RemedyRepack Inc. Due to Labeling: Incorrect...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Rocuronium Bromide 50 MG/5ML INJ. Recalled by RemedyRepack Inc. Due to...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Lorazepam 2 mg/mL Inj. Recalled by RemedyRepack Inc. Due to Labeling:...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Humulin 70/30 Recalled by RemedyRepack Inc. Due to Labeling: Incorrect...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 11, 2015· ConvaTec, Inc

Recalled Item: Nebulizer Masks Opti-Mist and Opti-Mist Clear Nebulizer masks are intended...

The Issue: The Nebulizer mask malfunctions in that there is reduced or no aerosol...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care" CCRP TestPak-in vitro diagnostic product intended to...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care CKMB DilPak- an in vitro diagnostic product Recalled by...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care DDMR TestPak Catalog Number: CDDMRE SMN: 10701511...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care MYO DilPak Catalog Number: CMYO-D SMN:10445081 in...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing